January 2023 | CMS MedTech

Medical Device Registration in UK

By cmsmedtech January 27, 2023UK

Authority for Medical Device Manufacturers must register their devices with the Medicines and Healthcare products Regulatory Agency (MHRA) before placing them onto the Great Britain market. Medical Device Definition “medical…

Medical Device Registration in New Zealand

By cmsmedtech January 13, 2023New Zealand

Authority for Medical Device Medsafe Medical Device Definition Legal Definition of a Medical Devicemeans any device, instrument, apparatus, appliance, or other article that -is intended to be used in, on,…

EU Authorised Representative

By cmsmedtech January 13, 2023CE, EC REP

In which cases do you need to assign the EU Authorised Representative for Medical Devices? Read further to know more about this subject. Certification Company – Your reliable EU Authorised Representative…

EU Medical Device Regulations

By cmsmedtech January 13, 2023CE1 Comment

What is EU-MDR compliance? The European Medical Device Regulation (MDR) is a set of regulations that governs the production and distribution of medical devices in Europe, and compliance with the…

MEDICAL DEVICE REGISTRATION IN AUSTRALIA

By cmsmedtech January 12, 2023Australia

Authority for Medical Device Therapeutic Goods Administration (TGA) is responsible for evaluating, assessing and monitoring medical devices to help Australians stay healthy and safe. Medical Device Definition Medical devices include…

Medical Device Registration in UK

Medical Device Registration in New Zealand

EU Authorised Representative

EU Medical Device Regulations

MEDICAL DEVICE REGISTRATION IN AUSTRALIA

EXTENSION OF THE MDR TRANSITIONAL PERIOD AND REMOVAL OF THE ‘SELL OFF’ PERIODS

Medical Device Registration in Thailand

Medical Device Registration Vietnam (updated 2023)

Medical Device Registration in UK

Medical Device Registration in New Zealand